U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

High density array fabrication and readout method for a fiber optic biosensor

Patent 5837196 Issued on November 17, 1998. Estimated Expiration Date: Icon_subject January 26, 2016. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

H1398

Fluorescent immunoassay employing optical fiber in capillary tube
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Inventor: Hirschfeld

Apparatus including optical fiber for fluorescence immunoassay
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Immunoassay apparatus
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Issued on: 03/20/1990
Inventor: Block, et al.

Waveguide-binding sensor for use with assays
Patent #: 5061857
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Inventor: Thompson, et al.

Fiber optic detector for immuno-testing
Patent #: 5082630
Issued on: 01/21/1992
Inventor: Partin, et al.

Method and apparatus for the regulation of complex binding
Patent #: 5135876
Issued on: 08/04/1992
Inventor: Andrade, et al.

Multiple optical fiber event sensor and method of manufacture
Patent #: 5166990
Issued on: 11/24/1992
Inventor: Riccitelli, et al.

Optical biosensor and method of use
Patent #: 5194393
Issued on: 03/16/1993
Inventor: Hugl, et al.

Imaging fiber optic array sensors, apparatus, and methods for concurrently detecting multiple analytes of interest in a fluid sample
Patent #: 5244636
Issued on: 09/14/1993
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Inventors

Assignee

Application

No. 592779 filed on 01/26/1996

US Classes:

422/55, Structured visual or optical indicator, per se65/409, Having plural adjacent fibers or rods sheathed (i.e., bundle) in tube or enclosure422/68.1, Means for analyzing liquid or solid sample422/82.05, Measuring optical property by using ultraviolet, infrared, or visible light422/82.06, Optode or optrode422/82.07, Fluorescence422/82.08, Fluorescence422/82.09, Absorbance or transmittance435/5, Involving virus or bacteriophage435/6, Involving nucleic acid435/91.2, Acellular exponential or geometric amplification (e.g., PCR, etc.)524/716Carbohydrate or derivative, e.g., nitrocellulose, etc.

Examiners

Primary: Zitomer, Stephanie W.
Assistant: Fredman, Jeffrey

Attorney, Agent or Firm

Foreign Patent References

  • WO 93/18186 WO. 09/12/1993
  • WO 95/35505 WO. 12/12/1995

International Classes

G01N 021/00
G01N 015/06
G01N 021/29
C12Q 001/68

Abstract

The invention relates to the fabrication and use of biosensors comprising a plurality of optical fibers each fiber having attached to its "sensor end" biological "binding partners" (molecules that specifically bind other molecules to form a binding complex such as antibody-antigen, lectin-carbohydrate, nucleic acid-nucleic acid, biotin-avidin, etc.). The biosensor preferably bears two or more different species of biological binding partner. The sensor is fabricated by providing a plurality of groups of optical fibers. Each group is treated as a batch to attach a different species of biological binding partner to the sensor ends of the fibers comprising that bundle. Each fiber, or group of fibers within a bundle, may be uniquely identified so that the fibers, or group of fibers, when later combined in an array of different fibers, can be discretely addressed. Fibers or groups of fibers are then selected and discretely separated from different bundles. The discretely separated fibers are then combined at their sensor ends to produce a high density sensor array of fibers capable of assaying simultaneously the binding of components of a test sample to the various binding partners on the different fibers of the sensor array. The transmission ends of the optical fibers are then discretely addressed to detectors--such as a multiplicity of optical sensors. An optical signal, produced by binding of the binding partner to its substrate to form a binding complex, is conducted through the optical fiber or group of fibers to a detector for each discrete test. By examining the addressed transmission ends of fibers, or groups of fibers, the addressed transmission ends can transmit unique patterns assisting in rapid sample identification by the sensor.

Other References

  • Anderson et al. Fiber optic based biosensor: signal enhancement in a production model. Proceedings SPIE--The International Society for Optical Engineering, vol. 1648: 39-43. Jan. 23-24, 1992
  • Krug et al., Anal. Chim. Acta., 256(2): 263-268 (1992)
  • Blum et al. Anal Chim. Acta., 226(2): 331-336 (1989)
  • Blum et al. Anal. Lett., 21(5): 717-726 (1988)
  • Hlavay et al. Biosensors and Bioelectronics, 9(3): 189-195 (1994)
  • Kallioniemi et al. Science, 258: 818-821 (1992)
  • Marx et al. J. Intelligent Material Systems and Structures, 5(4): 447-454 (1994)
  • Myrick et al. Fluorescence microstructure using a laser/fiber optic profiler. Proceedings of SPIE--The International Society for Optical Engineering., v 1302: 336-345 Apr. 16-18 (1990)
  • Steinitz et al, "An improved method to create nitrocellulose particles suitable for the immobilization of antigen and antibody", J. Immunol. Meth. 187(1):171-177, Nov. 1995
  • Thomas, "Hybridization of denatured RNA and small DNA fragments transfered to nitrocellulose", Proc. Natl. Acad. Sci. 77(9):5201-5205, Sep. 198
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